ATE205092T1 - METHOD FOR PRODUCING HIGHLY WATER SOLUBLE CYCLODEXTRIN COMPLEXES - Google Patents
METHOD FOR PRODUCING HIGHLY WATER SOLUBLE CYCLODEXTRIN COMPLEXESInfo
- Publication number
- ATE205092T1 ATE205092T1 AT93101237T AT93101237T ATE205092T1 AT E205092 T1 ATE205092 T1 AT E205092T1 AT 93101237 T AT93101237 T AT 93101237T AT 93101237 T AT93101237 T AT 93101237T AT E205092 T1 ATE205092 T1 AT E205092T1
- Authority
- AT
- Austria
- Prior art keywords
- optionally substituted
- derivative
- highly water
- soluble cyclodextrin
- group
- Prior art date
Links
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical class O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 title abstract 6
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract 2
- 150000003839 salts Chemical class 0.000 abstract 4
- 150000002284 fumagillol derivatives Chemical class 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 2
- 229910052717 sulfur Chemical group 0.000 abstract 2
- 125000006020 2-methyl-1-propenyl group Chemical group 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 238000002347 injection Methods 0.000 abstract 1
- 239000007924 injection Substances 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 238000003860 storage Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
- A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
- A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nanotechnology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
The present invention provides 1) a method of producing a complex of a fumagillol derivative of the formula: <CHEM> wherein R<1> is hydrogen; R<2> is halogen, N(O)mR<5>R<6>, N + R<5>R<6>R<7>.X- or S(O)nR<5>, wherein R<5>, R<6> and R<7> are independently an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; X- is a counter anion; m is 0 or 1; n is an integer of 0 to 2; and R<5> and R<6> together with the adjacent nitrogen or sulfur atom may form an optionally substituted nitrogen- or sulfur-containing heterocyclic group which may form a condensed ring; or R<1> and R<2> are combined to represent a chemical bond; R<3> is 2-methyl-1-propenyl group or isobutyl group; A is oxygen or NR<8>, wherein R<8> is hydrogen or an optionally substituted lower alkyl or aryl group; and R<4> is hydrogen, an optionally substituted hydrocarbon group or an optionally substituted acyl group; or a physiologically acceptable salt thereof, with a highly water-soluble cyclodextrin derivative, which comprises mixing the fumagillol derivative or a physiologically acceptable salt thereof with the highly water-soluble cyclodextrin derivative into an aqueous solution, the concentration of the highly water-soluble cyclodextrin derivative being at about 100 mg/ml or more, and 2) the complex of the fumaggillol derivative (I) or physiologically acceptable salt thereof with the highly water-soluble cyclodextrin derivative obtained by the production method 1). The complex of the fumagillol derivative (I) or physiologically acceptable salt thereof with the highly water-soluble cyclodextrin derivative is highly soluble in water, highly stable in storage and can be used as a preparation for injection.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1523692 | 1992-01-30 | ||
| JP33202192 | 1992-12-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE205092T1 true ATE205092T1 (en) | 2001-09-15 |
Family
ID=26351355
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT93101237T ATE205092T1 (en) | 1992-01-30 | 1993-01-28 | METHOD FOR PRODUCING HIGHLY WATER SOLUBLE CYCLODEXTRIN COMPLEXES |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5536623A (en) |
| EP (1) | EP0555693B1 (en) |
| AT (1) | ATE205092T1 (en) |
| CA (1) | CA2088428A1 (en) |
| DE (1) | DE69330690T2 (en) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2210600A1 (en) * | 1996-07-17 | 1998-01-17 | Takashi Houkan | Inhibitor of tumor metastasis or recurrence |
| KR100357541B1 (en) * | 1998-05-15 | 2002-10-18 | 주식회사종근당 | 5-Demthoxyfumagillol derivatives and processes for preparing the same |
| KR100357542B1 (en) * | 1998-05-15 | 2002-10-18 | 주식회사종근당 | Fumagillol derivatives and preparation method thereof |
| JP4922507B2 (en) * | 2000-08-10 | 2012-04-25 | 武田薬品工業株式会社 | Pharmaceutical composition |
| CA2418224C (en) | 2000-08-10 | 2010-02-09 | Takeda Chemical Industries, Ltd. | Pharmaceutical composition |
| KR100451485B1 (en) * | 2002-03-28 | 2004-10-06 | 주식회사종근당 | Inclusion compounds of fumagillol derivative or its salt, and pharmaceutical compositions comprising the same |
| CA2731020A1 (en) | 2008-07-18 | 2010-01-21 | Zafgen, Inc. | Use of antiangiogenic fumagillins in the treatment of obesity |
| WO2010065883A2 (en) | 2008-12-04 | 2010-06-10 | Zafgen Corporation | Method of treating an overweight or obese subject |
| US20120004162A1 (en) | 2008-12-04 | 2012-01-05 | Vath James E | Methods of Treating an Overweight or Obese Subject |
| MX337575B (en) | 2009-10-09 | 2016-03-10 | Zafgen Corp | SULFONE COMPOUNDS AND METHODS FOR THE MANUFACTURE AND USE OF THESE. |
| WO2011085198A1 (en) | 2010-01-08 | 2011-07-14 | Zafgen Corporation | Metap-2 inhibitor for use in treating benign prostatic hypertrophy (bph) |
| CN102791699B (en) | 2010-01-08 | 2016-04-06 | 扎夫根公司 | Aspergillus fumigatus alcohol type compound and its method of manufacture and use thereof |
| US20130266578A1 (en) | 2010-04-07 | 2013-10-10 | Thomas E. Hughes | Methods of treating an overweight subject |
| JP5913310B2 (en) | 2010-07-22 | 2016-04-27 | ザフゲン，インコーポレイテッド | Tricyclic compounds and methods of making and using the same |
| PH12013500934A1 (en) | 2010-11-09 | 2022-10-24 | Zafgen Inc | Crystalline solids of a metap-2 inhibitor and methods of making and using same |
| KR20140009273A (en) | 2010-11-29 | 2014-01-22 | 자프겐 인크. | Treatment of obesity using non-daily administration of 6-0-(4-dimethylaminoethoxy) cinnamoyl fumagillol |
| MX344238B (en) | 2011-01-26 | 2016-12-07 | Zafgen Inc | Tetrazole compounds and methods of making and using same. |
| BR112013023056A2 (en) | 2011-03-08 | 2018-10-09 | Zafgen Inc | oxospiro [2,5] octane derivatives and analogs |
| AU2012253760B2 (en) | 2011-05-06 | 2016-02-04 | Zafgen, Inc. | Tricyclic pyrazole sulfonamide compounds and methods of making and using same |
| MX343687B (en) | 2011-05-06 | 2016-11-16 | Zafgen Inc | Tricyclic sulfonamide compounds and methods of making and using same. |
| JP6062423B2 (en) | 2011-05-06 | 2017-01-18 | ザフゲン，インコーポレイテッド | Partially saturated tricyclic compounds and methods for their production and use |
| EP2763671A2 (en) | 2011-10-03 | 2014-08-13 | Zafgen, Inc. | Methods of treating age related disorders |
| WO2013109739A1 (en) | 2012-01-18 | 2013-07-25 | Zafgen, Inc. | Tricyclic sulfonamide compounds and methods of making and using same |
| KR20140112566A (en) | 2012-01-18 | 2014-09-23 | 자프겐 인크. | Tricyclic sulfone compounds and methods of making and using same |
| WO2013169727A1 (en) | 2012-05-07 | 2013-11-14 | Zafgen, Inc. | Polymorphic salt of the oxalate salt of 6 - o - ( 4 - dimethylaminoethoxy) cinnarnoyl fumagillol and methods of making and using same |
| JP2015516426A (en) | 2012-05-08 | 2015-06-11 | ザフゲン，インコーポレイテッド | Treatment of hypothalamic obesity with MetAP2 inhibitors |
| AU2013259620B2 (en) | 2012-05-09 | 2017-05-18 | Zafgen, Inc. | Fumigillol type compounds and methods of making and using same |
| JP2015536981A (en) | 2012-11-05 | 2015-12-24 | ザフゲン，インコーポレイテッド | Tricyclic compounds and methods for their production and use |
| WO2014071368A1 (en) | 2012-11-05 | 2014-05-08 | Zafgen, Inc. | Methods of treating liver diseases |
| CN104918928A (en) | 2012-11-05 | 2015-09-16 | 扎夫根股份有限公司 | Tricyclic compound and its preparation method and use |
| AU2014236528A1 (en) | 2013-03-14 | 2015-09-24 | Zafgen, Inc. | Methods of treating renal disease and other disorders |
| AR105671A1 (en) | 2015-08-11 | 2017-10-25 | Zafgen Inc | HUMEROCYCLIC COMPOUNDS OF FUMAGILLOL AND ITS METHODS OF ELABORATION AND USE |
| CN106432255A (en) | 2015-08-11 | 2017-02-22 | 扎夫根公司 | Fumigillol spiro-compound, preparation and use method thereof |
| CN113321753B (en) * | 2021-05-19 | 2022-08-30 | 山东滨州智源生物科技有限公司 | Preparation method of poly glycosyl amino acid cyclodextrin derivative and hydrogel |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0764884B2 (en) * | 1986-11-27 | 1995-07-12 | 株式会社トクヤマ | Cyclodextrin composition |
| JP2806454B2 (en) * | 1988-01-19 | 1998-09-30 | 武田薬品工業株式会社 | Angiogenesis inhibitor |
| DE68906942T3 (en) * | 1988-03-29 | 1999-05-12 | University Of Florida, Gainesville, Fla. | Pharmaceutical compositions for parenteral use. |
| US5227372A (en) * | 1990-03-07 | 1993-07-13 | Children's Medical Center Corporation | Method for retaining ophthalmological agents in ocular tissues |
| TW282399B (en) * | 1990-05-25 | 1996-08-01 | Takeda Pharm Industry Co Ltd | |
| ATE196426T1 (en) * | 1991-06-21 | 2000-10-15 | Takeda Chemical Industries Ltd | CYCLODEXTRIN COMPOSITION CONTAINING FUMAGILLOL DERIVATIVES |
-
1993
- 1993-01-28 EP EP93101237A patent/EP0555693B1/en not_active Expired - Lifetime
- 1993-01-28 AT AT93101237T patent/ATE205092T1/en active
- 1993-01-28 DE DE69330690T patent/DE69330690T2/en not_active Expired - Fee Related
- 1993-01-29 US US08/011,457 patent/US5536623A/en not_active Expired - Fee Related
- 1993-01-29 CA CA002088428A patent/CA2088428A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| DE69330690T2 (en) | 2002-06-20 |
| US5536623A (en) | 1996-07-16 |
| EP0555693A1 (en) | 1993-08-18 |
| DE69330690D1 (en) | 2001-10-11 |
| EP0555693B1 (en) | 2001-09-05 |
| CA2088428A1 (en) | 1993-07-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ATE205092T1 (en) | METHOD FOR PRODUCING HIGHLY WATER SOLUBLE CYCLODEXTRIN COMPLEXES | |
| ATE148993T1 (en) | CYCLODEXTRIN COMPLEX | |
| ATE71090T1 (en) | HETEROCYCLIC COMPOUNDS AND THEIR PREPARATION AND USE. | |
| JP3673888B2 (en) | Method for producing porphyrin metal complex | |
| ATE145209T1 (en) | TRI-AZA MACROCYCLES AND METHOD FOR THE PRODUCTION THEREOF | |
| KR910004630A (en) | 4-Methylene-2-oxo-8-azaspiro [4,5] decane derivatives and pharmaceutical compositions containing the compounds and methods of making them | |
| ATE138571T1 (en) | USE OF DIOXABICYCLO (3.3.0>OCTANE DERIVATIVES FOR THE PRODUCTION OF A DRUG FOR INHIBITING CHOLESTEROL METABOLISM. | |
| Lydon et al. | Synthesis and characterization of coordinated disulfides. Single-crystal structural analysis of [(en) 2Co (S (SC (CH3) 2COOH) C (CH3) 2COO)](ClO4) 2. cntdot. H2O | |
| DE69013528D1 (en) | A compound containing a perfluoroalkyl group. | |
| Derek | Kinetics of aminolysis of some benzoyl fluorides and benzoic anhydrides in non-hydroxylic solvents | |
| DE60026725D1 (en) | METHOD FOR THE PRODUCTION OF OPTICALLY ACTIVE NAPHTHALINE DERIVATIVES AND OPTICAL RESOLVERS THEREOF | |
| DE3885115D1 (en) | Process for the preparation of thiols. | |
| ATE122343T1 (en) | TRIAZOLYL HYDRAZIDE DERIVATIVES AND METHOD FOR THE PRODUCTION THEREOF. | |
| RO92245A (en) | PROCESS FOR THE PREPARATION OF 1,6-NAPHTHYRIDINE DERIVATIVES | |
| KR880001645A (en) | Method for preparing therapeutically useful pristine mycin | |
| ATE215934T1 (en) | NEW HISTIDE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS ANTI-FREE RADICAL AGENT | |
| HU895522D0 (en) | Process for the preparation of new thienyl-oxy-alkyl-amine derivatives and pharmaceutical compositions containing them | |
| KR890000406A (en) | Cinnamoylamide derivatives, methods for their preparation, pharmaceutical compositions containing them and their use | |
| Santos et al. | Siderophore analogues. Chelating properties of a new cyclic diazadihydroxamic acid | |
| KR900014305A (en) | Use of naphthalene methaneamino derivatives as anti-inflammatory agents and pharmaceutical compositions containing them | |
| SE9802643D0 (en) | 2,3-Disubstituted cyclopentanone derivatives, process for its preparation and medical use thereof | |
| KR910006238A (en) | Pyraz-3-carboxamide | |
| AR008257A1 (en) | WEATHER-STABLE POLYAMIDES AND PROCESS FOR THEIR PREPARATION AND APPLICATION | |
| IL106692A (en) | AZIDOALKYL DERIVATIVES AND THEIR USE FOR THE PREPARATION OF 99mTc COMPLEXES FOR IMAGING | |
| KR880012564A (en) | Benzimidazole derivatives and preparation method thereof |